Alogenuri organici

3-Amino-4-fluorobenzoic acid is a hydrocarbon that is used as an analgesic. It has been shown to be nontoxic and has analgesic effects in the intestinal tract. 3-Amino-4-fluorobenzoic acid also has radiopaque properties, which makes it useful for diagnosis and treatment of certain types of cancer and other tumors. The analgesic effect of 3-amino-4-fluorobenzoic acid may be due to its ability to act as a competitive antagonist at the N -methyl--aspartate (NMDA) receptor, which is important in pain perception.

4-Iodo-1-methyl-1H-imidazole is a trifluoroethylamine that inhibits the activity of tyrosine kinases. It binds to the active site of tyrosine kinase and prevents the binding of ATP, preventing phosphorylation and activation of downstream substrates. 4-Iodo-1-methyl-1H-imidazole has been shown to inhibit the proliferation of tumor xenografts in mice, as well as inhibiting headgroup binding and cellular proliferation in vitro. This agent also has a nanomolar range and high selectivity for protein kinases, which may make it suitable for therapeutic purposes.

5-Bromo-2-hydroxybenzaldehyde is an organic compound with a chemical formula of CHBrO. It is a white solid that is soluble in water, ethanol, and acetone. The synthesis of 5-bromo-2-hydroxybenzaldehyde has been achieved by the acylation reaction of benzaldehyde with bromide ion. The selectivity for this reaction can be increased by using sodium borohydride as a reducing agent instead of lithium aluminum hydride. This method can be applied to the synthesis of salmeterol, which is used as a medicine in the treatment of asthma.

Please enquire for more information about BNP-45 (mouse) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about H-Arg(Pmc)-2-chlorotrityl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-(Bromomethyl)-3-chlorobenzonitrile is a radioactive compound that has no specific use. It is used for the production of butylamino, which is a precursor to various other compounds. 4-(Bromomethyl)-3-chlorobenzonitrile can be used as an unlabelled replacement for any other radioactive compound in a laboratory setting.

4-Chloro-3-nitroaniline is an antibacterial agent that inhibits bacterial growth by binding to the enzyme topoisomerase II, which is essential for DNA replication. It has been shown to have a statistically significant inhibitory effect on the growth of Staphylococcus aureus. 4-Chloro-3-nitroaniline may also disrupt hemosiderosis and reduce iron levels in plasma samples from patients with hemosiderosis. The biological effects of this drug are not well understood.

3-Fluoro-2-nitrobenzaldehyde is a pyridine derivative that has been used in the synthesis of a number of important heterocyclic compounds. This compound can be prepared by reacting 3,4-dichloroaniline with nitrous acid and then hydrolyzing the resulting 3-chloroquinoline with hydrochloric acid. The reaction yields anilines and quinolines in regiospecifically, as well as formylation, cyclisation, and condensation products. It is also capable of aromatisation reactions with benzene to produce benzofuran derivatives.

Please enquire for more information about Suc-Ala-Phe-Lys-AMC trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

(Beta-Asp5)-delta-Sleep Inducing Peptide is a synthetic molecule that has been shown to be an atypical compound. It is a fragment of the natural sleep-inducing peptide, which is also called clostridium sporogenes. The fragment was synthesized and found to have similar properties and structures as the natural form. The fragment is labile in neutral or acidic solution, but stable in basic conditions. (Beta-Asp5)-delta-Sleep Inducing Peptide can be used for the detection of methyltransferase activity, by using it as a substrate for methylation reactions and measuring the rate of spontaneous desorption from a matrix. This compound can also be used for proteomic studies by using matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI TOF MS) techniques.

Please enquire for more information about H-Ser(tBu)-2-chlorotrityl resin (200-400 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page

N-(3-Bromopropyl)phthalimide is a chiral compound that can be used as a linker in the synthesis of ornithine. It is also an antibacterial agent. N-(3-Bromopropyl)phthalimide binds to the N-terminal amino group of ornithine and reacts with nucleophilic attack on the carbonyl carbon, forming the corresponding amide. The second-order rate constant for this reaction was measured to be 0.037 M-1s-1 at 25°C and pH 7. Photosensitizers such as silver nitrate are added to react with N-(3-bromopropyl)phthalimide and generate reactive oxygen species (ROS), which leads to surface-enhanced Raman scattering (SERS). SERS has been shown to be a useful technique for detecting N-(3-bromopropyl)phthalimide in food products.

Please enquire for more information about (Cys47)-HIV-1 tat Protein (47-57) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page